Frontiers in Immunology (Dec 2024)

Soluble CD52 mediates immune suppression by human seminal fluid

  • Leonard C. Harrison,
  • Leonard C. Harrison,
  • Natalie L. Stone,
  • Natalie L. Stone,
  • Esther Bandala-Sanchez,
  • Esther Bandala-Sanchez,
  • Nicholas D. Huntington,
  • Nicholas D. Huntington,
  • Robert I. McLachlan,
  • Jai Rautela,
  • Jai Rautela,
  • Moira K. O’Bryan

DOI
https://doi.org/10.3389/fimmu.2024.1497889
Journal volume & issue
Vol. 15

Abstract

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Seminal fluid provides for the carriage and nutrition of sperm, but also modulates immunity to prevent allo-rejection of sperm by the female. Immune suppression by seminal fluid has been associated with extracellular vesicles, originally termed prostasomes, which contain CD52, a glycosylated glycophosphoinositol-anchored peptide released from testicular epithelial cells. Previously, we reported that human T cell-derived CD52, bound to the danger-associated molecular pattern protein, high mobility group box 1 (HMGB1), suppresses T cell function via the inhibitory sialic acid-binding immunoglobulin-like lectin-10 (Siglec-10) receptor. Here we show that human seminal fluid contains high concentrations of CD52 complexed with HMGB1, which mediates T cell suppression indirectly via Siglec-7 on antigen-presenting cells. Proliferation of natural killer (NK) cells, which express Siglec-7 and play a key role in the immune defence of the uterus, was directly suppressed by seminal fluid CD52. These findings elucidate a critical function of seminal fluid to suppress cellular immunity and facilitate reproduction.

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